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Structural study of aqueous solutions of tetrahydrofuran and acetone mixtures using dielectric relaxation technique

机译:介电弛豫技术研究四氢呋喃和丙酮混合物水溶液的结构

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The complex permittivity, static dielectric constant and relaxation time for tetra-hydrofuran-water and acetone-water mixtures have been determined at 0°, 10°, 25° and 35℃ using time domain reflectometry technique (TDR). The behaviour of relaxation time of the mixture shows a maxima for the mixture with 30% of water by volume. This suggests that the tendency to form cluster between water and solute molecule is maximum for this mixture. The excess permittivity for both tetrahydrofuran-water mixture and acetone-water mixtures, are found to be negative. The Kirkwood correlation factor has been determined at various concentrations of water. Static dielectric constant for the mixtures have been fitted well with the modified Bruggeman model. The values of the Bruggeman parameter a for tetrahydrofuran is found to be more than the corresponding value for acetone.
机译:使用时域反射法(TDR)在四,六,三氢呋喃-水和丙酮-水的混合物中确定了复介电常数,静态介电常数和弛豫时间。混合物的弛豫时间行为表现出具有30体积%水的混合物的最大值。这表明该混合物在水和溶质分子之间形成簇的趋势最大。发现四氢呋喃-水混合物和丙酮-水混合物的过量介电常数均为负。柯克伍德相关系数已在各种浓度的水中测定。混合物的静态介电常数已与改进的Bruggeman模型很好地拟合。发现四氢呋喃的Bruggeman参数a的值大于丙酮的相应值。

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